A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14212145



Internal ID4213961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73203052..73203993hg38UCSC Ensembl
Innerchr11:73203053..73203993hg38UCSC Ensembl
Outerchr11:73203052..73203994hg38UCSC Ensembl
chr11:72914097..72915038hg19UCSC Ensembl
Innerchr11:72914098..72915038hg19UCSC Ensembl
Outerchr11:72914097..72915039hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626811
Supporting Variants
SamplesNA19185
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14212145
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer